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PRAS40是雷帕霉素复合物1的哺乳动物靶点,是该复合物下游信号传导所必需的。

PRAS40 is a target for mammalian target of rapamycin complex 1 and is required for signaling downstream of this complex.

作者信息

Fonseca Bruno D, Smith Ewan M, Lee Vivian H-Y, MacKintosh Carol, Proud Christopher G

机构信息

Department of Biochemistry and Molecular Biology, University of British Columbia, Vancouver, British Columbia V6T 1Z3, Canada.

出版信息

J Biol Chem. 2007 Aug 24;282(34):24514-24. doi: 10.1074/jbc.M704406200. Epub 2007 Jun 29.

Abstract

Signaling through the mammalian target of rapamycin complex 1 (mTORC1) is positively regulated by amino acids and insulin. PRAS40 associates with mTORC1 (which contains raptor) but not mTORC2. PRAS40 interacts with raptor, and this requires an intact TOR-signaling (TOS) motif in PRAS40. Like TOS motif-containing proteins such as eIF4E-binding protein 1 (4E-BP1), PRAS40 is a substrate for phosphorylation by mTORC1. Consistent with this, starvation of cells of amino acids or treatment with rapamycin alters the phosphorylation of PRAS40. PRAS40 binds 14-3-3 proteins, and this requires both amino acids and insulin. Binding of PRAS40 to 14-3-3 proteins is inhibited by TSC1/2 (negative regulators of mTORC1) and stimulated by Rheb in a rapamycin-sensitive manner. This confirms that PRAS40 is a target for regulation by mTORC1. Small interfering RNA-mediated knockdown of PRAS40 impairs both the amino acid- and insulin-stimulated phosphorylation of 4E-BP1 and the phosphorylation of S6. However, this has no effect on the phosphorylation of Akt or TSC2 (an Akt substrate). These data place PRAS40 downstream of mTORC1 but upstream of its effectors, such as S6K1 and 4E-BP1.

摘要

通过哺乳动物雷帕霉素靶蛋白复合物1(mTORC1)的信号传导受到氨基酸和胰岛素的正向调节。PRAS40与mTORC1(包含 Raptor)结合,但不与mTORC2结合。PRAS40与Raptor相互作用,这需要PRAS40中完整的TOR信号(TOS)基序。像含TOS基序的蛋白质如真核翻译起始因子4E结合蛋白1(4E-BP1)一样,PRAS40是mTORC1磷酸化的底物。与此一致,氨基酸饥饿或用雷帕霉素处理细胞会改变PRAS40的磷酸化。PRAS40结合14-3-3蛋白,这需要氨基酸和胰岛素两者。PRAS40与14-3-3蛋白的结合受到TSC1/2(mTORC1的负调节因子)的抑制,并以雷帕霉素敏感的方式受到Rheb的刺激。这证实PRAS40是mTORC1调节的靶点。小干扰RNA介导的PRAS40敲低损害了氨基酸和胰岛素刺激的4E-BP1磷酸化以及S6的磷酸化。然而,这对Akt或TSC2(一种Akt底物)的磷酸化没有影响。这些数据表明PRAS40在mTORC1的下游,但在其效应器如S6K1和4E-BP1的上游。

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